MQ TECHNICIAN III

TE Connectivity Corporation; Galway; On-site; EUR 42,000 - 62,000; Full time

Benefits offered by this job

33% shift allowance

Job summary

TE Connectivity Corporation in Galway, Ireland, is seeking a Quality/Manufacturing specialist for night shift. The role focuses on ensuring product and process quality, implementing corrective actions, and supporting audits to ISO and FDA standards.

Required are a Level 6 degree in Science/Engineering/Quality Management and 1+ year in manufacturing. Expect 33% shift allowance and involvement in quality control programs and documentation updates.

Qualifications

• Level 6 degree in Science/Engineering/Quality Management or related field is desirable.
• Industry experience in manufacturing is preferred.

Responsibilities

• Promote health and safety goals with Manufacturing teams.
• Deliver on KPIs to help the business achieve its goals.
• Implement corrective actions and determine root cause analysis.
• Audit procedures and ensure closure of findings.
• Support documentation, including Change plans and procedures.
• Provide support for internal, customer and regulatory audits (ISO/FDA).

Skills

Problem solving

Medical device quality systems

Product inspection techniques

Root cause analysis

FDA/ISO quality systems

Organizational skills

Communication skills

MS Word

MS Excel

MS PowerPoint

Education

Level 6 degree in Science/Engineering/Quality Management

Tools

MS Word

MS Excel

MS PowerPoint

Job description

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.

Job Description:

Job Overview

TE Connectivity’s Quality and Engineering Teams analyze the ability of product and production systems to comply with customer and contractual requirements through established reliability factors.

This role is based in balloons on the night shift: Monday - Thursday (4x 7 Hour Shifts) 12.15anm - 7.15am & Friday (11 Hour Shift) 6.15am - 5.15pm. There is a 33% shift allowance for this role.

They design, recommend revisions and install quality control systems, develop and document analytical methods for establishing reliability of products and their components and conduct analysis on relative reliability with regards to cost, structure, weight, maintainability, facility of production, and availability of materials and equipment. Out teams develop, implement and monitor company environmental safety programs and policies to ensure compliance with federal, state, and local environmental, health and safety regulations and recommend corrective actions if necessary.

They are responsible for policies and practices to comply with applicable government regulations and industry requirements related to product environmental compliance, the implementation and management of technical and testing standards and specifications, quality control and reliability programs governing materials, product and processes, resulting in the optimization of material and labor, as well as failure analysis, root cause, corrective action and customer communication.

Job Responsibilities

• Working with the Manufacturing teams promote the achievement of the Health and safety goals.
• Deliver on all KPIs that help the business achieve its goal.
• Implement corrective action on issues as they arise.
• Disposition non-conformances’, conduct & determine root cause analysis including corrective actions.
• Conduct area practice v’s procedure/Good Documentation Practice audits and follow up on findings to ensure satisfactory closure.
• Follow up on Corrective Actions for in-process and customer complaint issues.
• In-process sampling and testing and subsequent report writing.
• Conduct First Article Inspections on product as required.
• Processing procedure changes.
• Support all QA related documentation activities (i.e. Raise Change plans, write procedures etc).
• Review of sterilisation documentation and the release of sterilised product for shipping.
• Support functional area validation activities.
• Support Fault Analysis and Scrap Reduction activities.
• Participate/drive quality improvement projects/activities.
• Participate in preparing & on-going maintenance of FMEAs and Control Plans. Reporting function Quality metrics.
• Support NPI/manufacturing operations area projects and initiatives e,g, Kaizen, yield improvement, cost reduction etc.
• Other tasks as directed by the functional area Quality Engineer in line with company goals and objectives.
• Provide support for internal, customer and external audits to ISO and FDA requirements.
• Train operators on work instruction and procedural updates.

Qualifications

• Level 6 degree in Science / Engineering / Quality Management or related fields is desirable.
• Minimum of 1 years’ industry experience in a manufacturing environment.

Key Requirements

• A problem-solving qualification (either Green or Yellow belt) desirable.
• Clear understanding of medical device quality systems and requirements.
• Experience in product inspection techniques.
• Knowledge of root cause analytical and problem-solving skills.
• Knowledge of FDA and ISO Quality systems for Medical Device companies desirable.
• Demonstrated excellent organizational skills and ability to work on own initiative essential.
• Excellent written and verbal communication skills essential.
• Computer literate, MS Word, Excel, PowerPoint.

Job Locations

PARKMORE WEST
GALWAY, Galway H91 VN2T
Ireland